US20090191411A1 - Cycloaliphatic Polyester Copolymer Articles And Methods for Making Articles Therefrom - Google Patents

Cycloaliphatic Polyester Copolymer Articles And Methods for Making Articles Therefrom Download PDF

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US20090191411A1
US20090191411A1 US12/020,683 US2068308A US2009191411A1 US 20090191411 A1 US20090191411 A1 US 20090191411A1 US 2068308 A US2068308 A US 2068308A US 2009191411 A1 US2009191411 A1 US 2009191411A1
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sheet
polycarbonate
bis
polymer
combination
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Sandeep Tripathi
Shreyas Chakravarti
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SABIC Global Technologies BV
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SABIC Innovative Plastics IP BV
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Priority to US12/020,683 priority Critical patent/US20090191411A1/en
Assigned to SABIC INNOVATIVE PLASTICS IP B.V. reassignment SABIC INNOVATIVE PLASTICS IP B.V. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: CHAKRAVARTI, SHREYAS, TRIPATHI, SANDEEP
Assigned to CITIBANK, N.A., AS COLLATERAL AGENT reassignment CITIBANK, N.A., AS COLLATERAL AGENT SECURITY AGREEMENT Assignors: SABIC INNOVATIVE PLASTICS IP B.V.
Priority to TW98101782A priority patent/TWI399290B/zh
Priority to EP20090705086 priority patent/EP2242648B1/en
Priority to PCT/US2009/031569 priority patent/WO2009097209A2/en
Priority to CN200980103359.9A priority patent/CN102123864B/zh
Assigned to CITIBANK, N.A., AS COLLATERAL AGENT reassignment CITIBANK, N.A., AS COLLATERAL AGENT SECURITY AGREEMENT Assignors: SABIC INNOVATIVE PLASTICS IP B.V.
Publication of US20090191411A1 publication Critical patent/US20090191411A1/en
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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
    • B32B27/365—Layered products comprising a layer of synthetic resin comprising polyesters comprising polycarbonates
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2250/00—Layers arrangement
    • B32B2250/02—2 layers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2250/00—Layers arrangement
    • B32B2250/24—All layers being polymeric
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2270/00—Resin or rubber layer containing a blend of at least two different polymers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/40—Properties of the layers or laminate having particular optical properties
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/50—Properties of the layers or laminate having particular mechanical properties
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/50—Properties of the layers or laminate having particular mechanical properties
    • B32B2307/536—Hardness
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/50—Properties of the layers or laminate having particular mechanical properties
    • B32B2307/558—Impact strength, toughness
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/50—Properties of the layers or laminate having particular mechanical properties
    • B32B2307/582—Tearability
    • B32B2307/5825—Tear resistant
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/70—Other properties
    • B32B2307/714—Inert, i.e. inert to chemical degradation, corrosion
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/70—Other properties
    • B32B2307/738—Thermoformability
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/70—Other properties
    • B32B2307/75—Printability
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2307/00—Properties of the layers or laminate
    • B32B2307/70—Other properties
    • B32B2307/762—Self-repairing, self-healing
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2451/00—Decorative or ornamental articles
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2457/00—Electrical equipment
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B2509/00—Household appliances
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31507—Of polycarbonate

Definitions

  • thermoplastic films are gaining wide acceptance in applications such as household consumer electronics, appliances, and printed overlays. These applications demand a combination of properties such as clarity, printability, thermoformability, and hardness, as well as scratch, chemical, and impact resistance. This combination is not attainable with many materials of choice.
  • the most common solution has been to apply a functional coating as a cap layer on thermoplastic films, wherein the coating offers the surface properties while the base film provides the bulk mechanical integrity.
  • scratch resistance it takes away the films thermoformability, which seriously restricts the useful applications for such a film.
  • One of the most difficult challenges is the balance between scratch resistance and thermoformability remains.
  • thermoformable sheet can comprise: a cap layer comprising a combination of a bisphenol cyclohexylidene polycarbonate and a cycloaliphatic polyester copolymer, and a base layer comprising polycarbonate.
  • the sheet can comprise: a cap layer and a base layer comprising polycarbonate, wherein the sheet is thermoformable.
  • the cap layer can comprise a combination of a bisphenol cyclohexylidene polycarbonate and a second polymer, where the second polymer comprises 1,1-bis(4-hydroxy-3-methylphenyl)cyclohexane and poly(1,4-cyclohexane-dimethanol-1,4-dicarboxylate).
  • a method for making an article can comprise: melting a polycarbonate in an extruder, forming a molten combination of a bisphenol cyclohexylidene polycarbonate and a cycloaliphatic polyester copolymer, and coextruding the molten combination and the polycarbonate to form a sheet
  • FIG. 1 is a cross-sectional illustration of a scratch created by a profile load.
  • FIG. 2 is a schematic of an exemplary co-extrusion system.
  • Multilayer articles comprising a cap layer and a base layer.
  • the base layer comprises polycarbonate, polyester, polycarbonate copolymers, or a combination comprising at least one of the foregoing.
  • the cap layer comprises a combination of a bisphenol cyclohexylidene polycarbonate and a second polymer, where the second polymer is a cycloaliphatic polyester copolymer.
  • the cap layer and base layer can be coextruded to form a multilayer sheet.
  • Hardness, scratch resistance, mechanical strength, and thermoformability of such articles should enable these articles to meet a desired combination of properties such as clarity, printability, thermoformability, and hardness, as well as scratch, chemical, and impact resistance. Additionally, the base layer adheres to the cap layer without the need for any adhesive or a tie layer, and provides a substantial rheology match between the cap layer and the base layer, thereby improving the processability of the composite film.
  • thermoformable sheet can comprise: a cap layer comprising a combination of a bisphenol cyclohexylidene polycarbonate and a cycloaliphatic polyester copolymer, and a base layer comprising polycarbonate.
  • the amount of the second polymer can be 10 to 50 wt %, with the remainder being bisphenol cyclohexylidene polycarbonate.
  • the cycloaliphatic polyester copolymers can comprise at least 50 mole % cycloaliphatic residues, the remainder being the aromatic acid or C 1-4 alkylene glycol residues, or, specifically, at least 70 mole % cycloaliphatic residues.
  • the cycloaliphatic polyester copolymer can comprises 25 wt % to 100 wt % cycloaliphatic polyester, balance polycarbonate, or, specifically, 50 wt % to 90 wt % cycloaliphatic polyester.
  • the sheet can comprise a pencil hardness of greater than or equal to HB.
  • the sheet can comprise a tear initiation strength of greater than or equal to 120 N/mm, and/or a tear propagation strength of greater than or equal to 5 N/mm.
  • the sheet can be one that passes a formability test and/or a trimming test, wherein the formability test comprises preheating to 140° C.
  • the trimming test comprises trimming the formed part using matched metal dies comprising a hardened male die half and a hardened female die half, with a clearance between the male die half and female die half of 10% of sheet thickness; wherein the part is at a 90 degree angle to the blade at the time of impact. Combinations of the above properties and/or materials are also contemplated.
  • the sheet can comprise: a cap layer and a base layer comprising polycarbonate, wherein the sheet is thermoformable.
  • the cap layer can comprise a combination of a bisphenol cyclohexylidene polycarbonate and a second polymer, where the second polymer comprises 1,1-bis(4-hydroxy-3-methylphenyl)cyclohexane and poly(1,4-cyclohexane-dimethanol-1,4-dicarboxylate).
  • the second polymer can comprise less than or equal to 90 wt % of a combination of 1,1-bis(4-hydroxy-3-methylphenyl)cyclohexane and polycarbonate, based upon a total weight of the second polymer, or specifically, 50 wt % to 90 wt % of the combination of 1,1-bis(4-hydroxy-3-methylphenyl)cyclohexane and polycarbonate.
  • a method for making an article can comprise: melting a polycarbonate in an extruder, forming a molten combination of a bisphenol cyclohexylidene polycarbonate and a cycloaliphatic polyester copolymer, and coextruding the molten combination and the polycarbonate to form a sheet.
  • the sheet can be thermoformed.
  • the base layer comprises an aromatic polycarbonate comprising repeating structural units of the formula:
  • each R 1 is a C 6-30 aromatic group, that is, contains at least one aromatic moiety.
  • each R 1 is derived from a bisphenol compound of the formula (2):
  • R a and R b each represent a halogen or C 1-12 alkyl group and can be the same or different; and p and q are each independently integers of 0 to 4. It will be understood that R a is hydrogen when p is 0, and likewise R b is hydrogen when q is 0. Also in formula (2), X a represents a bridging group connecting the two hydroxy-substituted aromatic groups, where the bridging group and the hydroxy substituent of each C 6 arylene group are disposed ortho, meta, or para (specifically para) to each other on the C 6 arylene group.
  • the bridging group Xa is single bond, —O—, —S—, —S(O)—, —S(O) 2 —, —C(O)—, or a C 1-18 organic group.
  • the C 1-18 organic bridging group can be cyclic or acyclic, aromatic or non-aromatic, and can further comprise heteroatoms such as halogens, oxygen, nitrogen, sulfur, silicon, or phosphorous.
  • the C 1-18 organic group can be disposed such that the C 6 arylene groups connected thereto are each connected to a common alkylidene carbon or to different carbons of the C 1-18 organic bridging group.
  • p and q is each 1, and R a and R b are each a C 1-3 alkyl group, specifically methyl, disposed meta to the hydroxy group on each arylene group.
  • aromatic dihydroxy compounds include the following: 4,4′-dihydroxybiphenyl, 1,6-dihydroxynaphthalene, 2,6-dihydroxynaphthalene, bis(4-hydroxyphenyl)methane, bis(4-hydroxyphenyl)diphenylmethane, bis(4-hydroxyphenyl)-1-naphthylmethane, 1,2-bis(4-hydroxyphenyl)ethane, 1,1-bis(4-hydroxyphenyl)-1-phenylethane, 2-(4-hydroxyphenyl)-2-(3-hydroxyphenyl)propane, bis(4-hydroxyphenyl)phenylmethane, 2,2-bis(4-hydroxy-3-bromophenyl)propane, 1,1-bis(hydroxyphenyl)cyclopentane, 1,1-bis(4-hydroxyphenyl)cyclohexane, 1,1-bis(4-hydroxyphenyl)isobutene, 1,1
  • bisphenol compounds of formula (2) include 1,1-bis(4-hydroxyphenyl)methane, 1,1-bis(4-hydroxyphenyl)ethane, 2,2-bis(4-hydroxyphenyl)propane (hereinafter “bisphenol A” or “BPA”), 2,2-bis(4-hydroxyphenyl)butane, 2,2-bis(4-hydroxyphenyl)octane, 1,1-bis(4-hydroxyphenyl)propane, 1,1-bis(4-hydroxyphenyl)n-butane, 2,2-bis(4-hydroxy-1-methylphenyl)propane, 1,1-bis(4-hydroxy-t-butylphenyl)propane, 3,3-bis(4-hydroxyphenyl)phthalimidine, 2-phenyl-3,3-bis(4-hydroxyphenyl)phthalimidine (PPPBP), and 1,1-bis(4-hydroxy-3-methylphenyl)cyclohexane (DMBPC). Combinations comprising at least one of the for
  • the polycarbonate is a linear homopolymer derived from bisphenol A, in which p and q is each 0 and each of Y 1 is isopropylidene in formula (2).
  • the cap layer comprises a combination of bisphenol cyclohexylidene polycarbonate(s), a second polymer, where the second polymer comprises a cycloaliphatic polyester copolymer, and optionally additional polymer(s).
  • second polymers are set forth in commonly assigned U.S. patent application Ser. No. 11/177,134 to Geert Boven et al. and U.S. patent application Ser. No. 11/560,642 to Chaluavarti et al.
  • Bisphenol cyclohexylidene polycarbonates are of the formula (3):
  • each R 2 is derived from a bisphenol compound of formula (3) wherein R a , R b , p, and q are as defined above, at least a portion of the X a groups are cyclohexylidene, and the balance thereof are represented by groups of the formulas:
  • R c and R d each independently represent a hydrogen atom or a monovalent linear or cyclic C 1-12 hydrocarbon group and R e is a divalent hydrocarbon group.
  • R 2 groups are derived from a cyclohexylidene-bridged, alkyl-substituted bisphenol of formula (4)
  • R a′ and R b′ are each independently C 1-12 alkyl, R g is C 1-12 alkyl or halogen, r and s are each independently 1 to 4, and t is 0 to 10.
  • at least one of each of R a′ and R b′ are disposed meta to the cyclohexylidene bridging group.
  • the substituents R a , R b , and R g can, when comprising an appropriate number of carbon atoms, be straight chain, cyclic, bicyclic, branched, saturated, or unsaturated.
  • R a′ and R b′ are each independently C 1-4 alkyl, R g is C 1-4 alkyl, r and are each 1, and t is 0 to 5. In another specific embodiment, R a′ , R b′ and R g are each methyl, r and s are each 1, and t is 0 or 3.
  • the cyclohexylidene-bridged bisphenol can be the reaction product of two moles of o-cresol with one mole of cyclohexanone.
  • the cyclohexylidene-bridged bisphenol is the reaction product of two moles of a cresol with one mole of a hydrogenated isophorone (e.g., 1,1,3-trimethyl-3-cyclohexane-5-one).
  • a hydrogenated isophorone e.g., 1,1,3-trimethyl-3-cyclohexane-5-one.
  • DMBPC 1,1-bis(4-hydroxy-3-methylphenyl)cyclohexane
  • the bisphenol cyclohexylidene polycarbonates can be a homopolycarbonate (e.g., a DMBPC-containing homopolycarbonate) or a copolycarbonate wherein R 2 is derived from a cyclohexylidene-bridged bisphenol and another compound, e.g., 1,1-bis(4-hydroxyphenyl)methane, 1,1-bis(4-hydroxyphenyl)ethane, bisphenol A, 2,2-bis(4-hydroxyphenyl)butane, 2,2-bis(4-hydroxyphenyl)octane, 1,1-bis(4-hydroxyphenyl)propane, 1,1-bis(4-hydroxyphenyl)n-butane, 2,2-bis(4-hydroxy-1-methylphenyl)propane, 1,1-bis(4-hydroxy-t-butylphenyl)propane, 3,3-bis(4-hydroxyphenyl)phthalimidine, 2-phenyl-3,3-bis(4
  • the cap layer comprises a second polymer, where the second polymer can comprise a cycloaliphatic polyester copolymer.
  • the cycloaliphatic polyesters can have the formula (5):
  • R 13 and R 14 are independently at each occurrence an aryl, aliphatic or cycloalkane having 2 to 20 carbon atoms, with the proviso that at least one of R 13 and R 14 is a cycloaliphatic group.
  • the cycloaliphatic polyester is a condensation product where R 13 is the residue of a diol or a chemical equivalent thereof and R 14 is residue of a diacid or a chemical equivalent thereof.
  • both R 13 and R 14 are cycloalkyl-containing groups.
  • R 13 and R 14 are cycloalkyl radicals independently selected from the following structural units:
  • the diol is 1,4-cyclohexane dimethanol or a chemical equivalent thereof. Either or both of the cis or trans isomers of the 1,4-cyclohexane dimethanol can be used.
  • Chemical equivalents to the diols include esters, such as C 1-4 dialkylesters, diaryl esters, and the like.
  • Specific non-limiting examples of diacids include decahydro naphthalene dicarboxylic acids, norbornene dicarboxylic acids, bicyclo octane dicarboxylic acids, 1,4-cyclohexanedicarboxylic acid or the chemical equivalents thereof.
  • the diacids include trans-1,4-cyclohexanedicarboxylic acid or a chemical equivalent thereof.
  • Chemical equivalents of these diacids include C 1-4 dialkyl esters, diaryl esters, anhydrides, salts, acid chlorides, acid bromides, and the like.
  • the chemical equivalent comprises the dialkyl esters of the cycloaliphatic diacids, and most specifically the dimethyl ester of the acid, such as dimethyl-1,4-cyclohexane-dicarboxylate.
  • cycloaliphatic polyester copolymer examples include units derived from the reaction of an aromatic carboxylic diacid component and a non-cycloaliphatic diol, or chemical equivalents thereof.
  • aromatic dicarboxylic acids include isophthalic acid, terephthalic acid, 1,2-di(p-carboxyphenyl)ethane, 4,4′-dicarboxydiphenyl ether, 4,4′-bisbenzoic acid, 1,4-, 1,5-, or 2,6-naphthalenedicarboxylic acids, and combinations comprising at least one of the foregoing acids.
  • Specific dicarboxylic acids are terephthalic acid, isophthalic acid, and combinations comprising the two foregoing acids.
  • the non-cycloaliphatic diol can be a C 1-4 alkylene glycol, for example ethylene glycol, propylene glycol, 1,4-butylene glycol, and the like, and combinations comprising at least one of the foregoing glycols.
  • the cycloaliphatic polyester copolymers more specifically comprise at least 50 mole % of the cycloaliphatic residues, more specifically at least 70 mole % of the cycloaliphatic residues, the remainder being the aromatic acid or C 1-4 alkylene glycol residues.
  • a specific cycloaliphatic polyester is poly(cyclohexane-1,4-dimethylene cyclohexane-1,4-dicarboxylate), also referred to as poly(1,4-cyclohexane-dimethanol-1,4-dicarboxylate) (PCCD).
  • ester is poly(1,4-cyclohexylene dimethylene co-ethylene terephthalate) (PCTG) wherein greater than 50 mol % of the ester groups are derived from 1,4-cyclohexanedimethanol; and poly(ethylene-co-1,4-cyclohexylenedimethylene terephthalate) wherein greater than 50 mol % of the ester groups are derived from ethylene (PETG).
  • PCTG poly(1,4-cyclohexylene dimethylene co-ethylene terephthalate)
  • PETG poly(ethylene-co-1,4-cyclohexylenedimethylene terephthalate) wherein greater than 50 mol % of the ester groups are derived from ethylene (PETG).
  • PCTG poly(1,4-cyclohexylene dimethylene co-ethylene terephthalate)
  • PETG poly(ethylene-co-1,4-cyclohexylenedimethylene terephthalate) wherein greater than 50 mol % of the ester
  • the relative amount of the bisphenol cyclohexylidene polycarbonate and the second polymer varies with the specific application.
  • the amount of the second polymer is 10 wt % to 50 wt %, or, specifically, 20 wt % to 40 wt %, with the remainder being bisphenol cyclohexylidene polycarbonate.
  • the base layer composition is commercially available from GE Plastics as XYLEX®.
  • the base layer and/or cap layer can, independently, include various additives, with the proviso that the additives are selected so as to not significantly adversely affect the desired properties of the layers, for example, thermoformability, scratch resistance, and so forth.
  • additives can be used. Such additives can be mixed at a suitable time during the mixing of the components for forming the composition for each of the layers.
  • Possible additive(s) include as anti-oxidants, flame retardants, drip retardants, dyes, pigments, colorants, stabilizers (e.g., thermal, ultraviolet, and so forth), small particle mineral (such as clay, mica, and/or talc), antistatic agents, plasticizers, lubricants, mold release agents, whitening agents, reinforcing fillers (e.g., glass), and combinations comprising at least one of the foregoing.
  • the amount of additive(s) can be less than or equal to about 20 wt %, or, specifically, about 0.1 wt % to about 10 wt % additive(s), or, more specifically, about 0.25 wt % to about 5 wt % additive(s), based upon a total weight of the layer comprising the additive(s).
  • the present cap layer and base layer are formed by coextrusion.
  • the multi-layer composite can be suitably formed using a continuous calendaring co-extrusion process as shown schematically in FIG. 2 .
  • single screw extruders 1 and 2 supply resin melts for the individual layers (i.e., the top layer, the second layer and any additional polymeric layers) into a feed block 3.
  • a die 4 forms a molten polymeric web that is fed to a 3 roll-calendaring stack 5.
  • the calendaring stack comprises 2 to 4 counter-rotating cylindrical rolls with each roll, individually, made from metal (e.g., steel) or rubber coated metal. Each roll can be heated or cooled, as is appropriate.
  • the molten web formed by the die can be successively squeezed between the calendaring rolls.
  • the inter-roll clearances or “nips” through which the web is drawn determines the thickness of the layers.
  • the multi-layer composite may also be formed from separate pre-formed films corresponding to the polymeric layers which are subsequently laminated together, for example using heated rolls and optionally adhesive tie layers.
  • the layers can be coextruded to form various cap layer thickness percentage (i.e., cap layer thickness divided overall thickness).
  • the cap layer thickness percentage can be 1% to 99%, or, specifically, 5% to 60%, or, more specifically, 10% to 30%.
  • the overall thickness of the sheet can be up to and even exceeding several millimeters. More specifically, the sheet can have a thickness (e.g., gage) of 1 mil (25.4 micrometers ( ⁇ m)) to 500 mils (12,700 ⁇ m), or, yet more specifically, about 5 mils (127 ⁇ m) to about 40 mils (1016 ⁇ m), and yet more specifically, about 7 mils (178 ⁇ m) to about 30 mils (762 ⁇ m).
  • Bilayer films of varying cap layer compositions and film constructions were prepared using the coextrusion method described in relation to FIG. 2 .
  • the specific process parameters for each sample varied with individual layer thicknesses and the overall film thickness, the range of process parameters encompassing all samples in Table 2 is given in Table 3. It is understood that the process window for extruding these films is not restricted to that listed in Table 3.
  • An objective of this experiment was to determine whether or not there exists “a” condition at which these coextruded films could be made, i.e. whether or not these films are extrudable. Table 3 merely provides one set of conditions for co-extruding these films.
  • This example demonstrates the suitability of the disclosed articles for in mold decoration (IMD) applications.
  • Films for such applications should be amenable to the three sub-processes of IMD: (a) extrudability—ability to make films out of the selected materials, at a surface quality comparable to commercially available polished graphic films (e.g., Lexan 8010 film); (b) formability—ability to draw the films into different geometries; and (c) trimming—ability to cut the film cleanly without inducing any cracking or delamination.
  • Table 1 contains the chemical description and the source of the resins used in the film constructions set forth in Table 2.
  • Table 2 evaluates the samples along the above 3 attribute metrics: surface quality, thermoformability, and trimming.
  • surface quality 10 pieces of size 12 inches ⁇ 12 inches (30.5 cm ⁇ 30.5 cm) were examined by 3 operators to identify any imperfection (lines, dents, bumps) of length scales greater than 2 mm. Absence, to the unaided eye, of any such imperfection was considered a “pass”. It was not intended to test the optical quality of the films, but instead meant to identify any gross imperfections suggesting any issues with film co-extrusion.
  • thermoformed parts were trimmed using matched metal dies comprising hardened male and female die halves (American Iron and Steel Institute “AISI” Type A2 steel), with a clearance between the male die half and female die half of 10% of sheet thickness; wherein the part is at a 90 degree angle to the blade at the time of impact. Trimming the thermoformed part is an integral step in the IMD process. Multilayer structures with poor interlayer adhesion tend to delaminate during this step. A pass on this test is absence of any visible signs of cracking and any visible delamination during this step, with visibility determined with an unaided eye.
  • AISI American Iron and Steel Institute
  • the DMBPC-PC/PCCD blends remain ductile all the way up to 90% DMBPC-PC composition.
  • blending DMBPC-PC with BPA-PC in proportion greater than 85% makes the film too brittle, hence unsuitable for IMD processing.
  • This example demonstrates hardness and scratch resistance of the multilayer film.
  • Two samples were prepared in accordance with the film and resin composition set forth in Table 4. These samples were prepared the same way as those of Example 1.
  • a 2 layer coextruded polycarbonate film The cap is a PC copolymer while the base is PC (specifically Lexan ML 9735 commercially available from SABIC Innovative Plastics, Pittsfield, Mass.) (Sample 25) (known as 1HD00, commercially available from SABIC Innovative Plastics); a monolayer polycarbonate (Sample 26) polycarbonate (Lexan 8010, commercially available from SABIC Innovative Plastics); and a coated polycarbonate film (Sample 27) comprising a curable silica coating on a base of polycarbonate (specifically Lexan 8010) (known as HP92S, commercially available from SABIC Innovative Plastics), all commercially available from SABIC Innovative Plastics. It must be noted that HP92S is a coated film which is not formable.
  • Table 5 demonstrates that pencil hardness (ASTM D3363-05) as high as 2H can be achieved, which is a unit higher than the hardest formable film available. Higher DMBPC-PC content in the entire composite results in higher hardness. However, as mentioned earlier, a balance is needed between hardness and ductility for practical applications, which is achieved using the specified cap layer and overall film composition. Even blending DMBPC-PC down to 60 wt % results in hardness above hard coated polycarbonate films. However increasing the proportion of DMBPC-PC beyond 85 wt % doesn't result in any further improvement of the composite hardness. Preferred composition range is thus greater than 60 wt % and less than 85 wt %. The pencil hardness tests are subjective with significant standard deviation. In the following examples we present more quantitative measures of scratch resistance.
  • the samples were also tested for scratch resistance using an Erichsen Scratch Tester Type 413, which complies with ISO 1518. Forces of 2 Newtons (N) and 4N were applied to a conical stylus with radius if 0.01 millimeter (mm), which result in an indentation being made on the part surface. The extent of the indentation is subsequently measured by a Dektak 6M profilometer and is reported as the height of the indentation measured from the bottom of the indentation to the sample surface.
  • FIG. 1 is an illustration of one such scratch and the corresponding measured cross profile showing the build-up around the scratch. Reported below are the instantaneous depth (depth during) of the profile at the point when the load reaches 25 milliNewtons (mN).
  • the sheet had a tear initiation strength of greater than or equal to 120 N/mm, specifically, greater than or equal to 150 N/mm, more specifically, greater than or equal to 200 N/mm, yet more specifically, greater than or equal to 220 N/mm, and even greater than or equal to 230 N/mm. Furthermore, the tear propagation strength of the sheet was of greater than or equal to 5 N/mm, specifically, greater than or equal to 8 N/mm, more specifically, greater than or equal to 10 N/mm. As can be seen from the above, disclosed herein is a hard film that substantially retains its tear properties. It is further noted that a Sample comprising 2-layers, PMMA over PC film, with 50% cap layer, and an overall thickness of 7 mils, had a tear initiation of 95 N/mm despite having 4H hardness.
  • Ranges disclosed herein are inclusive and combinable (e.g., ranges of “up to about 25 wt %, or, more specifically, about 5 wt % to about 20 wt %”, is inclusive of the endpoints and all inner values of the ranges of “about 5 wt % to about 25 wt %,” etc.).
  • “Combination” is inclusive of blends, mixtures, derivatives, alloys, reaction products, and so forth.
  • the terms “first,” “second,” and so forth, herein do not denote any order, quantity, or importance, but rather are used to distinguish one element from another, and the terms “a” and “an” herein do not denote a limitation of quantity, but rather denote the presence of at least one of the referenced item.
  • (meth)acrylate encompasses both acrylate and methacrylate groups.
  • Compounds are described using standard nomenclature. For example, any position not substituted by any indicated group is understood to have its valency filled by a bond as indicated, or a hydrogen atom.
  • a dash (“-”) that is not between two letters or symbols is used to indicate a point of attachment for a substituent. For example, —CHO is attached through carbon of the carbonyl group.

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  • Laminated Bodies (AREA)
  • Wrappers (AREA)
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